Performance measures in dose-finding experiments
In the early phases of a clinical trial, the main statistical target is to estimate percentiles in response variables in order to control toxicity and efficiency of new drugs or, even, new medical procedures. In this work we present tools to study the performance of adaptive designs in phases I or II of clinical trials. The combined study of inferential and ethical criteria is also considered. Finally, these tools are used in a simulation study that evaluates the performance of some relevant adaptive procedures.
Palabras clave / Keywords: adaptive designs optimal designs
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